Dynarex Povidone Iodine Surgical Scrub

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Dynarex Povidone Iodine Surgical Scrub
Generic name: POVIDONE IODINE SURGICAL SCRUB SOLUTION
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 6f053e55-cbf6-9072-e053-2991aa0a2edd
SPL ID: 275871a0-3174-c7fa-e063-6394a90ac014
Version: 4
Effective date: 2024-11-20
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:17

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Dynarex Povidone Iodine Surgical Scrub	openfda.brand_name
generic name		POVIDONE IODINE SURGICAL SCRUB SOLUTION	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-142-51	openfda.package_ndc
ndc	package	67777-142-61	openfda.package_ndc
ndc	package	67777-142-50	openfda.package_ndc
ndc	package	67777-142-60	openfda.package_ndc
ndc	product	67777-142	openfda.product_ndc
ndc11	package	67777014261	derived:openfda.package_ndc
ndc11	package	67777014250	derived:openfda.package_ndc
ndc11	package	67777014260	derived:openfda.package_ndc
ndc11	package	67777014251	derived:openfda.package_ndc
spl id		275871a0-3174-c7fa-e063-6394a90ac014	id
spl set id		6f053e55-cbf6-9072-e053-2991aa0a2edd	set_id
unii		85H0HZU99M	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do Not Use if allergic to iodine in the eyes Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.